International safety notice

Corrective action/Recall for adjustors (LLBL, LLBH) and controls (LLBC1-2) of certain lots of IMMULITE LBP Kit (LKLB), IMMULITE 2000 LBP Kit (L2KLB), IMMULITE 2500 LBP Kit (L5KLB) or of IMMULITE LBP Control Modul (LLBCM), Siemens

Germany / BfArM · DEU · Dec 28, 2010

Key facts

Title Corrective action/Recall for adjustors (LLBL, LLBH) and controls (LLBC1-2) of certain lots of IMMULITE LBP Kit (LKLB), IMMULITE 2000 LBP Kit (L2KLB), IMMULITE 2500 LBP Kit (L5KLB) or of IMMULITE LBP Control Modul (LLBCM), Siemens
Regulator Germany / BfArM
Country DEU
Brand adjustors (LLBL, LLBH) and controls (LLBC1-2) of certain lots of IMMULITE LBP Kit (LKLB), IMMULITE 2000 LBP Kit (L2KLB), IMMULITE 2500 LBP Kit (L5KLB) or of IMMULITE LBP Control Modul (LLBCM), Siemens
Manufacturer Corrective action/Recall for adjustors (LLBL, LLBH) and controls (LLBC1-2) of certain lots of IMMULITE LBP Kit (LKLB), IMMULITE 2000 LBP Kit (L2KLB), IMMULITE 2500 LBP Kit (L5KLB) or of IMMULITE LBP Control Modul (LLBCM), Siemens
Models IMMULITE®2500, IMMULITE1000, LLBC1-2, 973.927.2828, 07836, L5KLB, GPF-003-6, L2KLB, 2010-03-25
Date Dec 28, 2010
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices